Associate Director Pathology

Associate Director of Pathology supports drug molecule efficacy and safety studies across multiple therapeutic focus areas (TFAs). Provides Clinical Pathology support for GLP toxicology and PK studies of Regeneron molecules, managing Clinical Pathology support to selected TFAs and mentoring junior pathologists.

Typical day may include:
- Serve as a scientific leader supporting nonclinical drug development across multiple therapeutic areas.
- Work independently and with integrated discovery and development teams to interpret pharmacologic and toxicity findings and advance therapeutics through the pipeline.
- Determine and evaluate clinical pathology-related endpoints in pharmacology and toxicology studies to guide decision-making.
- Collaborate with anatomic pathologists, toxicologists, and researchers within Regeneron.
- Partner with CRO partners to provide scientific peer review of nonclinical safety studies.

You may be a fit if you have:
- Experience integrating clinical and anatomic pathology data.
- Experience with animal models of human diseases.
- Clear, concise oral and written communication skills.
- Demonstrated ability to contribute to cross-functional teams.
- Ability to contribute to scientific strategy, problem-solving, and understanding of pathology issues influencing drug development outcomes.

Required:
- DVM (or equivalent) with ACVP certification in Clinical Pathology (strong preference for PhD).
- Minimum 3 years interpreting GLP and non-GLP clinical pathology data in nonclinical studies and supporting discovery research in a pharma/biotech or CRO setting.

Preferred:
- PhD in a scientific field and/or Certification in Anatomic Pathology.

Application instructions:
- Apply now.